EXCEED THE SPACE _ROVIDED. Spinal cord receives information that originates in the peripheral nerve endings and in the supraspinal motor centers. This information is integrated and used for generating a proper motor response. How does spinal cord achieve this complex integration task? The specificity of motor functions is encoded in different motor neuron subtypes that innervate distinct muscle targets. Sandwiched between the incoming information and the motor output are a multitude of premotor interneurons. How these neurons process information is not understood. Most interneurons in the spinal cord and elsewhere in the vertebrate CNS have eluded analysis because of the lack of specific markers to identify them. In transgenic mice cre-recombinase based indelible markers provide an unparalleled opportunity to study these neurons in the embryonic and adult spinal cord. Developmental studies have identified transcription factors that are expressed in subsets of interneurons, for example Lhx3. Promoters of these genes are ideal candidates for targeting cre-recombinase to select interneuron subtypes. A cre-reporter can then introduce an indelible mark in these interneurons and facilitate their identification throughout development and in the adult spinal cord. Marked and lineally related interneurons provide an opportunity to test the role of transcription factors and cell-cell interactions in cell-fate specification during development and maturation during the postnatal life. The proposed experiments will use this strategy to mark the I progeny of the Lhx3+ lineage, determine the role of four transcription factors and notch-mediated cell-cell communication in cell-fate specification. Further, synaptic partners of the marked neurons tnd their neurotransmitter properties will be determined. The information generated from these ;tudies will further our understanding of the spinal motor circuits and the role of interneurons in the I '1 :ontrol of motor functions in health and disease. JERFORMANCE SITE(S) (organization, city, state) The University of Chicago Chicago, Illinois 60637 KEY PERSONNEL ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS045106-03
Application #
6835179
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Chen, Daofen
Project Start
2002-12-01
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2005-11-30
Support Year
3
Fiscal Year
2005
Total Cost
$362,188
Indirect Cost
Name
University of Chicago
Department
Biology
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
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